DOI: 10.1055/s-00034916

Nervenheilkunde

References

Sallinen R, Vihola A, Bachinski LL, Huoponen K, Haapasalo H, Hackman P. et al.
New methods for molecular diagnosis and demonstration of the (CCTG)n mutation in myotonic dystrophy type 2 (DM2).

Neuromuscul Disord 2004;
14: 274-83.

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